| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:44066204-44066270 | Common:1; Rare:15 | ||||
| chr11:46345310-46345469 | Common:1; Rare:59 | ||||
| chr11:46617225-46617585 | Common:5; Rare:99 | ||||
| chr11:46700561-46700842 | Common:1; Rare:71 | ||||
| chr11:47176849-47177171 | Common:1; Rare:133 | ||||
| chr11:47269953-47270166 | Common:1; Rare:72 | ||||
| chr11:47426423-47426653 | Rare:56 | ||||
| chr11:47565505-47565640 | Common:3; Rare:24 | ||||
| chr11:47578947-47579094 | Rare:76; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642473-47642713 | Rare:98 | ||||
| chr11:47848315-47848376 | Rare:35 | ||||
| chr11:57324890-57325162 | Common:1; Rare:85 | ||||
| chr11:57712178-57712621 | Common:9; Rare:148 | ||||
| chr11:59142667-59142945 | Common:1; Rare:50 | ||||
| chr11:60906507-60906787 | Rare:72 |